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2010 | 1 |
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X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations.
Nat Genet. 2006 May;38(5):528-30. doi: 10.1038/ng1779. Epub 2006 Apr 9.
Nat Genet. 2006.
PMID: 16604071
Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey.
Rohatgi S, Clark D, Kline AD, Jackson LG, Pie J, Siu V, Ramos FJ, Krantz ID, Deardorff MA.
Rohatgi S, et al.
Am J Med Genet A. 2010 Jul;152A(7):1641-53. doi: 10.1002/ajmg.a.33441.
Am J Med Genet A. 2010.
PMID: 20583156
Free PMC article.
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